FDA
Food and Drug Administration · Recall Z-3065-2026 · Aug 11, 2026Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
Baxter Healthcare Corporation
The hazard
A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI) remains. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model UDI-DI 05413765852428Model all serial numbersUPC 05413765852428Would you have heard about this one?
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Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.